Exosome component 3
Protein-coding gene in the species Homo sapiens From Wikipedia, the free encyclopedia
Exosome component 3, also known as EXOSC3, is a human gene, which is part of the exosome complex.[5]
Clinical significance
Mutations in EXOSC3 cause pontocerebellar hypoplasia and spinal motor neuron degeneration.[6]
References
Further reading
External links
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